Canonical Allele Identifier: CA496393150

Gene: CDH1

Linked Data

• COSMIC: COSM20837
• MyVariant Identifiers: chr16:g.68857394del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823491del , CM000678.2:g.68823491del	GRCh38
NC_000016.9:g.68857394del , CM000678.1:g.68857394del	GRCh37
NC_000016.8:g.67414895del	NCBI36
NG_008021.1:g.91200del , LRG_301:g.91200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2029del MANE Select	ENSP00000261769.4:p.Gln677LysfsTer2
ENST00000261769.9:c.2029del	ENSP00000261769.4:p.Gln677LysfsTer2
ENST00000422392.6:c.1846del	ENSP00000414946.2:p.Gln616LysfsTer2
ENST00000562118.1:n.247del
ENST00000562836.5:n.2100del
ENST00000566510.5:c.*695del	ENSP00000458139.1:n.*695del
ENST00000566612.5:c.*269del	ENSP00000454782.1:n.*269del
ENST00000611625.4:c.2092del	ENSP00000481063.1:p.Gln698LysfsTer2
ENST00000612417.4:c.1830+1372del	ENSP00000478360.1:n.1830+1372del
ENST00000621016.4:c.1865+1337del	ENSP00000480664.1:n.1865+1337del
NM_004360.3:c.2029del , LRG_301t1:c.2029del	NP_004351.1:p.Gln677LysfsTer2
XM_011523488.1:c.1294del	XP_011521790.1:p.Gln432LysfsTer2
XM_011523489.1:c.1294del	XP_011521791.1:p.Gln432LysfsTer2
NM_001317184.1:c.1846del	NP_001304113.1:p.Gln616LysfsTer2
NM_001317185.1:c.481del	NP_001304114.1:p.Gln161LysfsTer2
NM_001317186.1:c.64del	NP_001304115.1:p.Gln22LysfsTer2
NM_004360.4:c.2029del	NP_004351.1:p.Gln677LysfsTer2
NM_004360.5:c.2029del MANE Select	NP_004351.1:p.Gln677LysfsTer2
NM_001317184.2:c.1846del	NP_001304113.1:p.Gln616LysfsTer2
NM_001317185.2:c.481del	NP_001304114.1:p.Gln161LysfsTer2
NM_001317186.2:c.64del	NP_001304115.1:p.Gln22LysfsTer2